Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Emmanouel Hatzipantelis"'
Autor:
Maria Kourti, Emmanouel Hatzipantelis
Publikováno v:
Diagnostics, Vol 13, Iss 23, p 3515 (2023)
Advances in risk-directed therapy based on prognostic factors that include clinical, biologic, and genetic features of cancer in children have yielded improved and prolonged responses [...]
Externí odkaz:
https://doaj.org/article/b733c52c2b8f47aeb8ee586e61bddd4c
Publikováno v:
Diagnostics, Vol 13, Iss 17, p 2748 (2023)
Acute lymphoblastic leukemia (ALL) is the most common cancer in children and one of the success stories in cancer therapeutics. Risk-directed therapy based on clinical, biologic and genetic features has played a significant role in this accomplishmen
Externí odkaz:
https://doaj.org/article/9c657c8908e94d3f89523f870ce8720b
Autor:
Elpis Mantadakis, Ioannis Kopsidas, Susan Coffin, Gabriel Dimitriou, Despoina Gkentzi, Emmanouel Hatzipantelis, Aikaterini Kaisari, Antonis Kattamis, Eleni Kourkouni, Smaragda Papachristidou, Evgenia Papakonstantinou, Sophia Polychronopoulou, Emmanuel Roilides, Nikos Spyridis, Sotirios Tsiodras, Maria N. Tsolia, Grammatiki-Christina Tsopela, Theoklis Zaoutis, Athanasios Tragiannidis
Publikováno v:
Antimicrobial Stewardship & Healthcare Epidemiology, Vol 2 (2022)
Abstract Objective: We surveyed antimicrobials used in Greek pediatric hematology–oncology (PHO) and bone marrow transplant (BMT) units before and after an intervention involving education regarding the 2017 clinical practice guidelines (CPG) for
Externí odkaz:
https://doaj.org/article/e18ebb02169447f285ac5f41ac820930
Autor:
Chrysoula Margioula-Siarkou, Stamatios Petousis, Georgia Margioula-Siarkou, George Mavromatidis, Fotios Chatzinikolaou, Emmanouel Hatzipantelis, Frédéric Guyon, Konstantinos Dinas
Publikováno v:
Diagnostics, Vol 13, Iss 6, p 1080 (2023)
Background: Ovarian malignant tumours are rarely diagnosed in adolescents but may have a significant impact on their survival, future fertility and quality of life. The management of such cases is rather complex and requires expertise and careful pla
Externí odkaz:
https://doaj.org/article/0f308039c287420480ea59ae1b2f7a39
Autor:
Alkistis Adramerina, Nikoleta Printza, Emmanouel Hatzipantelis, Symeon Symeonidis, Labib Tarazi, Aikaterini Teli, Marina Economou
Publikováno v:
Biology, Vol 11, Iss 2, p 247 (2022)
Thalassemic syndromes are characterized by clinical heterogenicity. For severe disease forms, lifelong blood transfusions remain the mainstay of therapy, while iron overload monitoring and adequate chelation treatment are required in order to ensure
Externí odkaz:
https://doaj.org/article/4e7d4267738446138fb8e9ad05bf2ce9
Autor:
Maria Kourti, Emmanouel Hatzipantelis, Thomas Zaramboukas, Athanassios Tragiannides, Georgios Petrakis, Fani Athanassiadou-Piperopoulou
Publikováno v:
Rare Tumors, Vol 4, Iss 1, Pp e6-e6 (2012)
We report our institutional experience of the management of 2 cases of rare non-Wilms’ tumors; a rhabdoid tumor in a 17-month old boy and a clear cell sarcoma in a 5-year old girl. The two patients were treated with ifosfamide/ carboplatin/etoposid
Externí odkaz:
https://doaj.org/article/d3ed47dcebc64413afbef4d6d283840d
Autor:
Theodoros Theodoridis, Vassilios Achyropoulos, Georgios Mavromatidis, D Dovas, John N. Bontis, Fotios Goutzioulis, Konstantinos Dinas, Tantanasis T, Emmanouel Hatzipantelis, Leonidas Zepiridis
Publikováno v:
Acta Obstetricia et Gynecologica Scandinavica. 86:938-944
Recent studies have shown that gingivitis and periodontal infection during pregnancy represent an independent risk factor for pre-term birth. However, little is known about the prevalence and correlates of dental attendance during pregnancy.During th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f520b8e63fe2a28c773ef24657503510
https://doi.org/10.1080/00016340701371413
https://doi.org/10.1080/00016340701371413
Autor:
G. Petrakis, Maria Kourti, Thomas Zaramboukas, Emmanouel Hatzipantelis, Athanassios Tragiannidis, Fani Athanassiadou-Piperopoulou
Publikováno v:
Rare Tumors, Vol 4, Iss 1, Pp e6-e6 (2012)
Rare Tumors
Rare Tumors
We report our institutional experience of the management of 2 cases of rare non-Wilms’ tumors; a rhabdoid tumor in a 17-month old boy and a clear cell sarcoma in a 5-year old girl. The two patients were treated with ifosfamide/carboplatin/etoposide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::133db4c7f23aef0e2240626db58e2689
http://www.pagepress.org/journals/index.php/rt/article/view/2533
http://www.pagepress.org/journals/index.php/rt/article/view/2533
Autor:
Sidi, V., Fragandrea, I., EMMANOUEL HATZIPANTELIS, Kyriakopoulos, C., Papanikolaou, A., Bandouraki, M., Koliouskas, D. E.
Publikováno v:
Scopus-Elsevier
Alveolar soft– part sarcoma (ASPS) is a rare form of soft tissue sarcoma and is most often seen in adolescents and young adults. Surgical excision of the primary tumor and pulmonary metastases has resulted in prolonged survival in some patients whi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::24cb96575fc59bca76d9025326930ff0
https://europepmc.org/articles/PMC2580048/
https://europepmc.org/articles/PMC2580048/
Autor:
Georgios Mavromatidis, Konstantinos Dinas, Dimitrios Delkos, Fotios Goutzioulis, Christos Vosnakis, Emmanouel Hatzipantelis, Vassilia Garipidou, David Rousso
Publikováno v:
International journal of hematology. 86(3)
Factor XI (FXI) is a procoagulant factor and antifibrinolytic agent, and its absence causes a bleeding tendency. FXI deficiency is autosomal in inheritance, with severe FXI deficiency in homozygotes and partial deficiency in heterozygotes. A 24-year-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc65ea9a035ceafaa37808d55a81265c
https://pubmed.ncbi.nlm.nih.gov/17988987
https://pubmed.ncbi.nlm.nih.gov/17988987